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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs34427160

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr1:161221661-161221688 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
del(T)20 / del(T)18 / del(T)17 / d…

del(T)20 / del(T)18 / del(T)17 / del(T)15 / del(T)14 / del(T)13 / del(T)12 / del(T)11 / del(T)10 / del(T)9 / del(T)8 / del(T)7 / del(T)6 / del(T)5 / del(T)4 / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)4 / dup(T)5 / dup(T)6 / dup(T)7 / dup(T)8 / dup(T)9 / dup(T)10 / dup(T)15 / dup(T)16 / dup(T)17 / dup(T)18 / dup(T)19 / dup(T)20 / dup(T)23 / dup(T)24 / dup(T)25 / dup(T)26

Variation Type
Indel Insertion and Deletion
Frequency
del(T)7=0.0516 (341/6606, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
None
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 6606 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8804 TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0516, TTTTTTTTTTTTTTTTTTTTTT=0.0174, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0115, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0341, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0038, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000 0.909879 0.008319 0.081802 25
European Sub 6172 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.8723 TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0551, TTTTTTTTTTTTTTTTTTTTTT=0.0185, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0123, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0365, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0041, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000 0.902585 0.008992 0.088423 22
African Sub 244 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000 TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
African Others Sub 6 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0 TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0 1.0 0.0 0.0 N/A
African American Sub 238 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.000 TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000 1.0 0.0 0.0 N/A
Asian Sub 2 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0 TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0 1.0 0.0 0.0 N/A
East Asian Sub 0 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0 TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0 0 0 0 N/A
Other Asian Sub 2 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.0 TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0 1.0 0.0 0.0 N/A
Latin American 1 Sub 16 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00 TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Latin American 2 Sub 64 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00 TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
South Asian Sub 16 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=1.00 TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A
Other Sub 92 TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.98 TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00 1.0 0.0 0.0 N/A


Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
Allele Frequency Aggregator Total Global 6606 (T)28=0.8804 del(T)20=0.0000, del(T)18=0.0000, del(T)17=0.0000, del(T)15=0.0000, del(T)14=0.0000, del(T)13=0.0000, del(T)12=0.0000, del(T)11=0.0000, del(T)10=0.0000, del(T)9=0.0000, del(T)8=0.0000, del(T)7=0.0516, del(T)6=0.0174, del(T)5=0.0000, del(T)4=0.0000, delTTT=0.0115, delTT=0.0341, delT=0.0038, dupT=0.0000, dupTT=0.0000, dup(T)9=0.0012
Allele Frequency Aggregator European Sub 6172 (T)28=0.8723 del(T)20=0.0000, del(T)18=0.0000, del(T)17=0.0000, del(T)15=0.0000, del(T)14=0.0000, del(T)13=0.0000, del(T)12=0.0000, del(T)11=0.0000, del(T)10=0.0000, del(T)9=0.0000, del(T)8=0.0000, del(T)7=0.0551, del(T)6=0.0185, del(T)5=0.0000, del(T)4=0.0000, delTTT=0.0123, delTT=0.0365, delT=0.0041, dupT=0.0000, dupTT=0.0000, dup(T)9=0.0013
Allele Frequency Aggregator African Sub 244 (T)28=1.000 del(T)20=0.000, del(T)18=0.000, del(T)17=0.000, del(T)15=0.000, del(T)14=0.000, del(T)13=0.000, del(T)12=0.000, del(T)11=0.000, del(T)10=0.000, del(T)9=0.000, del(T)8=0.000, del(T)7=0.000, del(T)6=0.000, del(T)5=0.000, del(T)4=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)9=0.000
Allele Frequency Aggregator Other Sub 92 (T)28=0.98 del(T)20=0.00, del(T)18=0.00, del(T)17=0.00, del(T)15=0.00, del(T)14=0.00, del(T)13=0.00, del(T)12=0.00, del(T)11=0.00, del(T)10=0.00, del(T)9=0.00, del(T)8=0.00, del(T)7=0.01, del(T)6=0.01, del(T)5=0.00, del(T)4=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)9=0.00
Allele Frequency Aggregator Latin American 2 Sub 64 (T)28=1.00 del(T)20=0.00, del(T)18=0.00, del(T)17=0.00, del(T)15=0.00, del(T)14=0.00, del(T)13=0.00, del(T)12=0.00, del(T)11=0.00, del(T)10=0.00, del(T)9=0.00, del(T)8=0.00, del(T)7=0.00, del(T)6=0.00, del(T)5=0.00, del(T)4=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)9=0.00
Allele Frequency Aggregator Latin American 1 Sub 16 (T)28=1.00 del(T)20=0.00, del(T)18=0.00, del(T)17=0.00, del(T)15=0.00, del(T)14=0.00, del(T)13=0.00, del(T)12=0.00, del(T)11=0.00, del(T)10=0.00, del(T)9=0.00, del(T)8=0.00, del(T)7=0.00, del(T)6=0.00, del(T)5=0.00, del(T)4=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)9=0.00
Allele Frequency Aggregator South Asian Sub 16 (T)28=1.00 del(T)20=0.00, del(T)18=0.00, del(T)17=0.00, del(T)15=0.00, del(T)14=0.00, del(T)13=0.00, del(T)12=0.00, del(T)11=0.00, del(T)10=0.00, del(T)9=0.00, del(T)8=0.00, del(T)7=0.00, del(T)6=0.00, del(T)5=0.00, del(T)4=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)9=0.00
Allele Frequency Aggregator Asian Sub 2 (T)28=1.0 del(T)20=0.0, del(T)18=0.0, del(T)17=0.0, del(T)15=0.0, del(T)14=0.0, del(T)13=0.0, del(T)12=0.0, del(T)11=0.0, del(T)10=0.0, del(T)9=0.0, del(T)8=0.0, del(T)7=0.0, del(T)6=0.0, del(T)5=0.0, del(T)4=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dup(T)9=0.0
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 1 NC_000001.11:g.161221669_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221671_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221672_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221674_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221675_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221676_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221677_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221678_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221679_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221680_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221681_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221682_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221683_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221684_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221685_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221686_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221687_161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221688del
GRCh38.p14 chr 1 NC_000001.11:g.161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221687_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221686_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221685_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221684_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221683_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221682_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221681_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221680_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221679_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221674_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221673_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221672_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221671_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221670_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221669_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221666_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221665_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221664_161221688dup
GRCh38.p14 chr 1 NC_000001.11:g.161221663_161221688dup
GRCh37.p13 chr 1 NC_000001.10:g.161191459_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191461_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191462_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191464_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191465_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191466_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191467_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191468_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191469_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191470_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191471_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191472_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191473_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191474_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191475_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191476_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191477_161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191478del
GRCh37.p13 chr 1 NC_000001.10:g.161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191477_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191476_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191475_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191474_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191473_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191472_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191471_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191470_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191469_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191464_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191463_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191462_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191461_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191460_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191459_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191456_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191455_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191454_161191478dup
GRCh37.p13 chr 1 NC_000001.10:g.161191453_161191478dup
APOA2 RefSeqGene NG_012043.1:g.6949_6968del
APOA2 RefSeqGene NG_012043.1:g.6951_6968del
APOA2 RefSeqGene NG_012043.1:g.6952_6968del
APOA2 RefSeqGene NG_012043.1:g.6954_6968del
APOA2 RefSeqGene NG_012043.1:g.6955_6968del
APOA2 RefSeqGene NG_012043.1:g.6956_6968del
APOA2 RefSeqGene NG_012043.1:g.6957_6968del
APOA2 RefSeqGene NG_012043.1:g.6958_6968del
APOA2 RefSeqGene NG_012043.1:g.6959_6968del
APOA2 RefSeqGene NG_012043.1:g.6960_6968del
APOA2 RefSeqGene NG_012043.1:g.6961_6968del
APOA2 RefSeqGene NG_012043.1:g.6962_6968del
APOA2 RefSeqGene NG_012043.1:g.6963_6968del
APOA2 RefSeqGene NG_012043.1:g.6964_6968del
APOA2 RefSeqGene NG_012043.1:g.6965_6968del
APOA2 RefSeqGene NG_012043.1:g.6966_6968del
APOA2 RefSeqGene NG_012043.1:g.6967_6968del
APOA2 RefSeqGene NG_012043.1:g.6968del
APOA2 RefSeqGene NG_012043.1:g.6968dup
APOA2 RefSeqGene NG_012043.1:g.6967_6968dup
APOA2 RefSeqGene NG_012043.1:g.6966_6968dup
APOA2 RefSeqGene NG_012043.1:g.6965_6968dup
APOA2 RefSeqGene NG_012043.1:g.6964_6968dup
APOA2 RefSeqGene NG_012043.1:g.6963_6968dup
APOA2 RefSeqGene NG_012043.1:g.6962_6968dup
APOA2 RefSeqGene NG_012043.1:g.6961_6968dup
APOA2 RefSeqGene NG_012043.1:g.6960_6968dup
APOA2 RefSeqGene NG_012043.1:g.6959_6968dup
APOA2 RefSeqGene NG_012043.1:g.6954_6968dup
APOA2 RefSeqGene NG_012043.1:g.6953_6968dup
APOA2 RefSeqGene NG_012043.1:g.6952_6968dup
APOA2 RefSeqGene NG_012043.1:g.6951_6968dup
APOA2 RefSeqGene NG_012043.1:g.6950_6968dup
APOA2 RefSeqGene NG_012043.1:g.6949_6968dup
APOA2 RefSeqGene NG_012043.1:g.6946_6968dup
APOA2 RefSeqGene NG_012043.1:g.6945_6968dup
APOA2 RefSeqGene NG_012043.1:g.6944_6968dup
APOA2 RefSeqGene NG_012043.1:g.6943_6968dup
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement (T)28= del(T)20 del(T)18 del(T)17 del(T)15 del(T)14 del(T)13 del(T)12 del(T)11 del(T)10 del(T)9 del(T)8 del(T)7 del(T)6 del(T)5 del(T)4 delTTT delTT delT dupT dupTT dupTTT dup(T)4 dup(T)5 dup(T)6 dup(T)7 dup(T)8 dup(T)9 dup(T)10 dup(T)15 dup(T)16 dup(T)17 dup(T)18 dup(T)19 dup(T)20 dup(T)23 dup(T)24 dup(T)25 dup(T)26
GRCh38.p14 chr 1 NC_000001.11:g.161221661_161221688= NC_000001.11:g.161221669_161221688del NC_000001.11:g.161221671_161221688del NC_000001.11:g.161221672_161221688del NC_000001.11:g.161221674_161221688del NC_000001.11:g.161221675_161221688del NC_000001.11:g.161221676_161221688del NC_000001.11:g.161221677_161221688del NC_000001.11:g.161221678_161221688del NC_000001.11:g.161221679_161221688del NC_000001.11:g.161221680_161221688del NC_000001.11:g.161221681_161221688del NC_000001.11:g.161221682_161221688del NC_000001.11:g.161221683_161221688del NC_000001.11:g.161221684_161221688del NC_000001.11:g.161221685_161221688del NC_000001.11:g.161221686_161221688del NC_000001.11:g.161221687_161221688del NC_000001.11:g.161221688del NC_000001.11:g.161221688dup NC_000001.11:g.161221687_161221688dup NC_000001.11:g.161221686_161221688dup NC_000001.11:g.161221685_161221688dup NC_000001.11:g.161221684_161221688dup NC_000001.11:g.161221683_161221688dup NC_000001.11:g.161221682_161221688dup NC_000001.11:g.161221681_161221688dup NC_000001.11:g.161221680_161221688dup NC_000001.11:g.161221679_161221688dup NC_000001.11:g.161221674_161221688dup NC_000001.11:g.161221673_161221688dup NC_000001.11:g.161221672_161221688dup NC_000001.11:g.161221671_161221688dup NC_000001.11:g.161221670_161221688dup NC_000001.11:g.161221669_161221688dup NC_000001.11:g.161221666_161221688dup NC_000001.11:g.161221665_161221688dup NC_000001.11:g.161221664_161221688dup NC_000001.11:g.161221663_161221688dup
GRCh37.p13 chr 1 NC_000001.10:g.161191451_161191478= NC_000001.10:g.161191459_161191478del NC_000001.10:g.161191461_161191478del NC_000001.10:g.161191462_161191478del NC_000001.10:g.161191464_161191478del NC_000001.10:g.161191465_161191478del NC_000001.10:g.161191466_161191478del NC_000001.10:g.161191467_161191478del NC_000001.10:g.161191468_161191478del NC_000001.10:g.161191469_161191478del NC_000001.10:g.161191470_161191478del NC_000001.10:g.161191471_161191478del NC_000001.10:g.161191472_161191478del NC_000001.10:g.161191473_161191478del NC_000001.10:g.161191474_161191478del NC_000001.10:g.161191475_161191478del NC_000001.10:g.161191476_161191478del NC_000001.10:g.161191477_161191478del NC_000001.10:g.161191478del NC_000001.10:g.161191478dup NC_000001.10:g.161191477_161191478dup NC_000001.10:g.161191476_161191478dup NC_000001.10:g.161191475_161191478dup NC_000001.10:g.161191474_161191478dup NC_000001.10:g.161191473_161191478dup NC_000001.10:g.161191472_161191478dup NC_000001.10:g.161191471_161191478dup NC_000001.10:g.161191470_161191478dup NC_000001.10:g.161191469_161191478dup NC_000001.10:g.161191464_161191478dup NC_000001.10:g.161191463_161191478dup NC_000001.10:g.161191462_161191478dup NC_000001.10:g.161191461_161191478dup NC_000001.10:g.161191460_161191478dup NC_000001.10:g.161191459_161191478dup NC_000001.10:g.161191456_161191478dup NC_000001.10:g.161191455_161191478dup NC_000001.10:g.161191454_161191478dup NC_000001.10:g.161191453_161191478dup
APOA2 RefSeqGene NG_012043.1:g.6941_6968= NG_012043.1:g.6949_6968del NG_012043.1:g.6951_6968del NG_012043.1:g.6952_6968del NG_012043.1:g.6954_6968del NG_012043.1:g.6955_6968del NG_012043.1:g.6956_6968del NG_012043.1:g.6957_6968del NG_012043.1:g.6958_6968del NG_012043.1:g.6959_6968del NG_012043.1:g.6960_6968del NG_012043.1:g.6961_6968del NG_012043.1:g.6962_6968del NG_012043.1:g.6963_6968del NG_012043.1:g.6964_6968del NG_012043.1:g.6965_6968del NG_012043.1:g.6966_6968del NG_012043.1:g.6967_6968del NG_012043.1:g.6968del NG_012043.1:g.6968dup NG_012043.1:g.6967_6968dup NG_012043.1:g.6966_6968dup NG_012043.1:g.6965_6968dup NG_012043.1:g.6964_6968dup NG_012043.1:g.6963_6968dup NG_012043.1:g.6962_6968dup NG_012043.1:g.6961_6968dup NG_012043.1:g.6960_6968dup NG_012043.1:g.6959_6968dup NG_012043.1:g.6954_6968dup NG_012043.1:g.6953_6968dup NG_012043.1:g.6952_6968dup NG_012043.1:g.6951_6968dup NG_012043.1:g.6950_6968dup NG_012043.1:g.6949_6968dup NG_012043.1:g.6946_6968dup NG_012043.1:g.6945_6968dup NG_012043.1:g.6944_6968dup NG_012043.1:g.6943_6968dup
Help

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

86 SubSNP, 54 Frequency submissions
No Submitter Submission ID Date (Build)
1 ABI ss41145644 Mar 15, 2016 (147)
2 ABI ss41275243 Dec 03, 2013 (138)
3 HGSV ss82262910 Dec 15, 2007 (129)
4 HGSV ss82269094 Dec 15, 2007 (129)
5 HUMANGENOME_JCVI ss95244657 Mar 15, 2016 (147)
6 PJP ss294606960 May 09, 2011 (142)
7 EVA_UK10K_ALSPAC ss1701308291 Apr 01, 2015 (144)
8 EVA_UK10K_TWINSUK ss1701308366 Apr 01, 2015 (144)
9 EVA_UK10K_TWINSUK ss1709952744 Apr 01, 2015 (144)
10 EVA_UK10K_ALSPAC ss1709952748 Apr 01, 2015 (144)
11 SWEGEN ss2987827791 Nov 08, 2017 (151)
12 MCHAISSO ss3064426981 Nov 08, 2017 (151)
13 URBANLAB ss3646801354 Oct 11, 2018 (152)
14 EVA_DECODE ss3687874144 Jul 12, 2019 (153)
15 EVA_DECODE ss3687874145 Jul 12, 2019 (153)
16 EVA_DECODE ss3687874146 Jul 12, 2019 (153)
17 EVA_DECODE ss3687874147 Jul 12, 2019 (153)
18 EVA_DECODE ss3687874148 Jul 12, 2019 (153)
19 EVA_DECODE ss3687874149 Jul 12, 2019 (153)
20 ACPOP ss3727524728 Jul 12, 2019 (153)
21 ACPOP ss3727524729 Jul 12, 2019 (153)
22 ACPOP ss3727524730 Jul 12, 2019 (153)
23 PACBIO ss3783579421 Jul 12, 2019 (153)
24 PACBIO ss3789208657 Jul 12, 2019 (153)
25 PACBIO ss3794080685 Jul 12, 2019 (153)
26 PACBIO ss3794080686 Jul 12, 2019 (153)
27 EVA ss3826448199 Apr 25, 2020 (154)
28 FSA-LAB ss3983951341 Apr 25, 2021 (155)
29 GNOMAD ss4004548307 Apr 25, 2021 (155)
30 GNOMAD ss4004548308 Apr 25, 2021 (155)
31 GNOMAD ss4004548309 Apr 25, 2021 (155)
32 GNOMAD ss4004548310 Apr 25, 2021 (155)
33 GNOMAD ss4004548311 Apr 25, 2021 (155)
34 GNOMAD ss4004548312 Apr 25, 2021 (155)
35 GNOMAD ss4004548313 Apr 25, 2021 (155)
36 GNOMAD ss4004548314 Apr 25, 2021 (155)
37 GNOMAD ss4004548315 Apr 25, 2021 (155)
38 GNOMAD ss4004548316 Apr 25, 2021 (155)
39 GNOMAD ss4004548317 Apr 25, 2021 (155)
40 GNOMAD ss4004548318 Apr 25, 2021 (155)
41 GNOMAD ss4004548319 Apr 25, 2021 (155)
42 GNOMAD ss4004548320 Apr 25, 2021 (155)
43 GNOMAD ss4004548321 Apr 25, 2021 (155)
44 GNOMAD ss4004548322 Apr 25, 2021 (155)
45 GNOMAD ss4004548323 Apr 25, 2021 (155)
46 GNOMAD ss4004548324 Apr 25, 2021 (155)
47 GNOMAD ss4004548325 Apr 25, 2021 (155)
48 GNOMAD ss4004548326 Apr 25, 2021 (155)
49 GNOMAD ss4004548327 Apr 25, 2021 (155)
50 GNOMAD ss4004548328 Apr 25, 2021 (155)
51 GNOMAD ss4004548329 Apr 25, 2021 (155)
52 GNOMAD ss4004548330 Apr 25, 2021 (155)
53 GNOMAD ss4004548331 Apr 25, 2021 (155)
54 GNOMAD ss4004548332 Apr 25, 2021 (155)
55 GNOMAD ss4004548333 Apr 25, 2021 (155)
56 GNOMAD ss4004548334 Apr 25, 2021 (155)
57 GNOMAD ss4004548335 Apr 25, 2021 (155)
58 GNOMAD ss4004548336 Apr 25, 2021 (155)
59 GNOMAD ss4004548337 Apr 25, 2021 (155)
60 GNOMAD ss4004548338 Apr 25, 2021 (155)
61 GNOMAD ss4004548339 Apr 25, 2021 (155)
62 GNOMAD ss4004548340 Apr 25, 2021 (155)
63 TOMMO_GENOMICS ss5146697284 Apr 25, 2021 (155)
64 TOMMO_GENOMICS ss5146697285 Apr 25, 2021 (155)
65 TOMMO_GENOMICS ss5146697286 Apr 25, 2021 (155)
66 TOMMO_GENOMICS ss5146697287 Apr 25, 2021 (155)
67 TOMMO_GENOMICS ss5146697288 Apr 25, 2021 (155)
68 TOMMO_GENOMICS ss5146697289 Apr 25, 2021 (155)
69 1000G_HIGH_COVERAGE ss5244453325 Oct 12, 2022 (156)
70 1000G_HIGH_COVERAGE ss5244453326 Oct 12, 2022 (156)
71 1000G_HIGH_COVERAGE ss5244453327 Oct 12, 2022 (156)
72 HUGCELL_USP ss5445026018 Oct 12, 2022 (156)
73 HUGCELL_USP ss5445026019 Oct 12, 2022 (156)
74 HUGCELL_USP ss5445026020 Oct 12, 2022 (156)
75 HUGCELL_USP ss5445026021 Oct 12, 2022 (156)
76 HUGCELL_USP ss5445026022 Oct 12, 2022 (156)
77 EVA ss5623999106 Oct 12, 2022 (156)
78 EVA ss5623999107 Oct 12, 2022 (156)
79 TOMMO_GENOMICS ss5673959462 Oct 12, 2022 (156)
80 TOMMO_GENOMICS ss5673959463 Oct 12, 2022 (156)
81 TOMMO_GENOMICS ss5673959464 Oct 12, 2022 (156)
82 TOMMO_GENOMICS ss5673959465 Oct 12, 2022 (156)
83 TOMMO_GENOMICS ss5673959466 Oct 12, 2022 (156)
84 TOMMO_GENOMICS ss5673959467 Oct 12, 2022 (156)
85 EVA ss5832728746 Oct 12, 2022 (156)
86 EVA ss5832728747 Oct 12, 2022 (156)
87 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 2129367 (NC_000001.10:161191450:TTTTTTT: 718/3854)
Row 2129368 (NC_000001.10:161191451:TTTTT: 323/3854)

- Oct 11, 2018 (152)
88 The Avon Longitudinal Study of Parents and Children

Submission ignored due to conflicting rows:
Row 2129367 (NC_000001.10:161191450:TTTTTTT: 718/3854)
Row 2129368 (NC_000001.10:161191451:TTTTT: 323/3854)

- Oct 11, 2018 (152)
89 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
90 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
91 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
92 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
93 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
94 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
95 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
96 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
97 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
98 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
99 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
100 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
101 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
102 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
103 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
104 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
105 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
106 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
107 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
108 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
109 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
110 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
111 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
112 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
113 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
114 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
115 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
116 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
117 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
118 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
119 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
120 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
121 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
122 gnomAD - Genomes

Submission ignored due to conflicting rows:
Row 28409922 (NC_000001.11:161221660::T 424/85448)
Row 28409923 (NC_000001.11:161221660::TT 27/85472)
Row 28409924 (NC_000001.11:161221660::TTT 14/85474)...

- Apr 25, 2021 (155)
123 Northern Sweden

Submission ignored due to conflicting rows:
Row 809593 (NC_000001.10:161191450:TTTTTTT: 12/568)
Row 809594 (NC_000001.10:161191450::TTTTTTTTTTTTTTTTTTTTTTTT 4/568)
Row 809595 (NC_000001.10:161191450:TTTTTT: 2/568)

- Jul 12, 2019 (153)
124 Northern Sweden

Submission ignored due to conflicting rows:
Row 809593 (NC_000001.10:161191450:TTTTTTT: 12/568)
Row 809594 (NC_000001.10:161191450::TTTTTTTTTTTTTTTTTTTTTTTT 4/568)
Row 809595 (NC_000001.10:161191450:TTTTTT: 2/568)

- Jul 12, 2019 (153)
125 Northern Sweden

Submission ignored due to conflicting rows:
Row 809593 (NC_000001.10:161191450:TTTTTTT: 12/568)
Row 809594 (NC_000001.10:161191450::TTTTTTTTTTTTTTTTTTTTTTTT 4/568)
Row 809595 (NC_000001.10:161191450:TTTTTT: 2/568)

- Jul 12, 2019 (153)
126 8.3KJPN

Submission ignored due to conflicting rows:
Row 4666591 (NC_000001.10:161191450:TTTTTT: 3165/15656)
Row 4666592 (NC_000001.10:161191450:TTTTTTT: 3866/15656)
Row 4666593 (NC_000001.10:161191450:TTTTTTTT: 6/15656)...

- Apr 25, 2021 (155)
127 8.3KJPN

Submission ignored due to conflicting rows:
Row 4666591 (NC_000001.10:161191450:TTTTTT: 3165/15656)
Row 4666592 (NC_000001.10:161191450:TTTTTTT: 3866/15656)
Row 4666593 (NC_000001.10:161191450:TTTTTTTT: 6/15656)...

- Apr 25, 2021 (155)
128 8.3KJPN

Submission ignored due to conflicting rows:
Row 4666591 (NC_000001.10:161191450:TTTTTT: 3165/15656)
Row 4666592 (NC_000001.10:161191450:TTTTTTT: 3866/15656)
Row 4666593 (NC_000001.10:161191450:TTTTTTTT: 6/15656)...

- Apr 25, 2021 (155)
129 8.3KJPN

Submission ignored due to conflicting rows:
Row 4666591 (NC_000001.10:161191450:TTTTTT: 3165/15656)
Row 4666592 (NC_000001.10:161191450:TTTTTTT: 3866/15656)
Row 4666593 (NC_000001.10:161191450:TTTTTTTT: 6/15656)...

- Apr 25, 2021 (155)
130 8.3KJPN

Submission ignored due to conflicting rows:
Row 4666591 (NC_000001.10:161191450:TTTTTT: 3165/15656)
Row 4666592 (NC_000001.10:161191450:TTTTTTT: 3866/15656)
Row 4666593 (NC_000001.10:161191450:TTTTTTTT: 6/15656)...

- Apr 25, 2021 (155)
131 8.3KJPN

Submission ignored due to conflicting rows:
Row 4666591 (NC_000001.10:161191450:TTTTTT: 3165/15656)
Row 4666592 (NC_000001.10:161191450:TTTTTTT: 3866/15656)
Row 4666593 (NC_000001.10:161191450:TTTTTTTT: 6/15656)...

- Apr 25, 2021 (155)
132 14KJPN

Submission ignored due to conflicting rows:
Row 7796566 (NC_000001.11:161221660:TTTTTTT: 6534/24194)
Row 7796567 (NC_000001.11:161221660:TTTTTT: 5231/24194)
Row 7796568 (NC_000001.11:161221660:TTTTTTTT: 7/24194)...

- Oct 12, 2022 (156)
133 14KJPN

Submission ignored due to conflicting rows:
Row 7796566 (NC_000001.11:161221660:TTTTTTT: 6534/24194)
Row 7796567 (NC_000001.11:161221660:TTTTTT: 5231/24194)
Row 7796568 (NC_000001.11:161221660:TTTTTTTT: 7/24194)...

- Oct 12, 2022 (156)
134 14KJPN

Submission ignored due to conflicting rows:
Row 7796566 (NC_000001.11:161221660:TTTTTTT: 6534/24194)
Row 7796567 (NC_000001.11:161221660:TTTTTT: 5231/24194)
Row 7796568 (NC_000001.11:161221660:TTTTTTTT: 7/24194)...

- Oct 12, 2022 (156)
135 14KJPN

Submission ignored due to conflicting rows:
Row 7796566 (NC_000001.11:161221660:TTTTTTT: 6534/24194)
Row 7796567 (NC_000001.11:161221660:TTTTTT: 5231/24194)
Row 7796568 (NC_000001.11:161221660:TTTTTTTT: 7/24194)...

- Oct 12, 2022 (156)
136 14KJPN

Submission ignored due to conflicting rows:
Row 7796566 (NC_000001.11:161221660:TTTTTTT: 6534/24194)
Row 7796567 (NC_000001.11:161221660:TTTTTT: 5231/24194)
Row 7796568 (NC_000001.11:161221660:TTTTTTTT: 7/24194)...

- Oct 12, 2022 (156)
137 14KJPN

Submission ignored due to conflicting rows:
Row 7796566 (NC_000001.11:161221660:TTTTTTT: 6534/24194)
Row 7796567 (NC_000001.11:161221660:TTTTTT: 5231/24194)
Row 7796568 (NC_000001.11:161221660:TTTTTTTT: 7/24194)...

- Oct 12, 2022 (156)
138 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 2129367 (NC_000001.10:161191450:TTTTTTT: 742/3708)
Row 2129368 (NC_000001.10:161191451:TTTTT: 338/3708)

- Oct 11, 2018 (152)
139 UK 10K study - Twins

Submission ignored due to conflicting rows:
Row 2129367 (NC_000001.10:161191450:TTTTTTT: 742/3708)
Row 2129368 (NC_000001.10:161191451:TTTTT: 338/3708)

- Oct 11, 2018 (152)
140 ALFA NC_000001.11 - 161221661 Apr 25, 2021 (155)
Help

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID History Updated (Build)
rs60551943 Oct 26, 2010 (133)
rs144776973 Aug 21, 2014 (142)
Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT

(self)
ss4004548340 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT

(self)
ss4004548339 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

(self)
ss4004548338 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT

(self)
ss4004548337 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

(self)
ss4004548336 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT

(self)
ss4004548335 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT

(self)
ss4004548334 NC_000001.11:161221660:TTTTTTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

(self)
ss4004548333, ss5244453325, ss5445026022 NC_000001.11:161221660:TTTTTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT

(self)
ss4004548332 NC_000001.11:161221660:TTTTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT

(self)
ss3983951341, ss5146697286 NC_000001.10:161191450:TTTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
ss3646801354, ss3687874144, ss4004548331, ss5673959464 NC_000001.11:161221660:TTTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT

(self)
ss1701308291, ss1701308366, ss2987827791, ss3727524728, ss3826448199, ss5146697285, ss5623999107, ss5832728746 NC_000001.10:161191450:TTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
ss3064426981, ss4004548330, ss5445026020, ss5673959462 NC_000001.11:161221660:TTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
ss3687874145 NC_000001.11:161221661:TTTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT

(self)
ss3727524730, ss5146697284, ss5623999106, ss5832728747 NC_000001.10:161191450:TTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
ss1709952744, ss1709952748 NC_000001.10:161191451:TTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548329, ss5244453327, ss5445026021, ss5673959463 NC_000001.11:161221660:TTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
ss3687874146 NC_000001.11:161221662:TTTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT

(self)
NC_000001.10:161191451:TTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548328 NC_000001.11:161221660:TTTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT

(self)
ss5244453326 NC_000001.11:161221660:TTTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss5146697289 NC_000001.10:161191450:TTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548327, ss5445026018, ss5673959466 NC_000001.11:161221660:TTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3687874147 NC_000001.11:161221665:TTT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss82262910, ss82269094 NC_000001.8:158004549:TT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss294606960 NC_000001.9:159458100:TT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3794080685, ss5146697287 NC_000001.10:161191450:TT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss5673959465 NC_000001.11:161221660:TT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3687874148 NC_000001.11:161221666:TT: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3783579421, ss3789208657, ss3794080686, ss5146697288 NC_000001.10:161191450:T: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548326, ss5445026019, ss5673959467 NC_000001.11:161221660:T: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss41275243 NT_004487.19:12680118:T: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss41145644, ss95244657 NT_004487.19:12680119:T: NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548307 NC_000001.11:161221660::T NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3687874149 NC_000001.11:161221668::T NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548308 NC_000001.11:161221660::TT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548309 NC_000001.11:161221660::TTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548310 NC_000001.11:161221660::TTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548311 NC_000001.11:161221660::TTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548312 NC_000001.11:161221660::TTTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss95244657 NT_004487.19:12680119:T:TTTTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548313 NC_000001.11:161221660::TTTTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548314 NC_000001.11:161221660::TTTTTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548315 NC_000001.11:161221660::TTTTTTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
9845334068 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548316 NC_000001.11:161221660::TTTTTTTTTT NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548317 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548318 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548319 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548320 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548321 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548322 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548323 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss3727524729 NC_000001.10:161191450::TTTTTTTTTT…

NC_000001.10:161191450::TTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548324 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
ss4004548325 NC_000001.11:161221660::TTTTTTTTTT…

NC_000001.11:161221660::TTTTTTTTTTTTTTTTTTTTTTTTTT

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

(self)
Removed from this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Destination RSIDs
ss3093368572 NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTT:

NC_000001.11:161221660:TTTTTTTTTTT…

NC_000001.11:161221660:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT

Help

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34427160

Help

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
Top Help

NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post820+afb47a3d